✦ LIBER ✦

Synthesis of Sphingomyelin and Ceramide 1-Phosphate from Ceramide without Protection of the Allylic Hydroxyl Group

✍ Scribed by Byun, Hoe-Sup; Erukulla, Ravi Kumar; Bittman, Robert

Book ID: 121428999
Publisher: American Chemical Society
Year: 1994
Tongue: English
Weight: 531 KB
Volume: 59
Category: Article
ISSN: 0022-3263
DOI: 10.1021/jo00100a069

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Efficient synthesis of sphingosine-1-pho

Efficient synthesis of sphingosine-1-phosphate, ceramide-1-phosphate, lysosphingomyelin, and sphingomyelin

✍ Kratzer, Bernd ;Schmidt, Richard R. 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 English ⚖ 839 KB

## Abstract Readily available D‐__erythro__‐azidosphingosine is transformed into 3‐__O__‐silyl‐protected derivative 6. Reduction of the azido group afforded 3‐__O__‐silyl‐protected sphingosine 7 which was either converted into __N__‐Fmoc‐protected derivative 8 or via N‐acylation into ceramide deriv

Synthesis of a novel cyclic pentacovalen

Synthesis of a novel cyclic pentacovalent phosphoenol ether derived from a dienone. Approaches to the syntheses of phosphonate analogs of sphingomyelin, sphingosine 1-phosphate and ceramide 1-phosphate

✍ Cynthia K McClure; Pranab K Mishra 📂 Article 📅 2002 🏛 Elsevier Science 🌐 French ⚖ 180 KB

The synthesis of a new pentacovalent oxaphospholene from a dienone, and its use as an enolate equivalent in the approach toward the syntheses of phosphonate analogs of sphingomyelin, sphingosine 1-phosphate and ceramide 1-phosphate are described. Condensation of the new P(V) reagent with an azodicar

ChemInform Abstract: Synthetic Studies T

ChemInform Abstract: Synthetic Studies Toward the Preparation of Phosphonate Analogues of Sphingomyelin and Ceramide 1-Phosphate Using Pentacovalent Organophospholene Methodology.

✍ C. K. MCCLURE; P. K. MISHRA; C. W. GROTE 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB

THE PHOSPHATE-PHOSPHONATE AND PHOSPHONAT

THE PHOSPHATE-PHOSPHONATE AND PHOSPHONATE-PHOSPHATE REARRANGEMENTS AND THEIR APPLICATIONS - 7[1]: USE OF t -BUTYL AS PROTECTING GROUP AND SYNTHESIS OF CHIRAL, NONRACEMIC α-HYDROXYPHOSPHONATES

✍ Hammerschmidt, Friedrich; Schmidt, Susanne 📂 Article 📅 2001 🏛 Taylor and Francis Group 🌐 English ⚖ 742 KB

ESI-MS and MS/MS identification of the f

ESI-MS and MS/MS identification of the first ceramide analogues of fumonisin B 1 mycotoxin from a Fusarium verticillioides culture following RP-HPLC separation

✍ Bartók, T.; Szécsi, Á.; Juhász, K.; Bartók, M.; Mesterházy, Á. 📂 Article 📅 2013 🏛 Taylor and Francis Group 🌐 English ⚖ 574 KB

1,1,1,3,3,3-Hexafluoro-2-propanol for th

1,1,1,3,3,3-Hexafluoro-2-propanol for the removal of the 4,4′-DimethoxytrityI protecting group from the 5′-hydroxyl of acid-sensitive nucleosides and nucleotides

✍ Nelson J. Leonard; Neelima 📂 Article 📅 1995 🏛 Elsevier Science 🌐 French ⚖ 211 KB